Amobarbital, deficient n-hydroxylation of

Preferred Label : Amobarbital, deficient n-hydroxylation of;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %204800;

Details

Origin ID

204800;

UMLS CUI

C1859816;

Currated CISMeF NLP mapping
- amobarbital, deficient N-Hydroxylation of [MeSH concept]
- amobarbital, deficient N-Hydroxylation of [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Autosomal recessive inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- amobarbital, deficient N-Hydroxylation of [MeSH Supplementary Concept]
- amobarbital, deficient N-Hydroxylation of [MeSH concept]

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